Project Engineer

Sligo  ‐ Onsite
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Keywords

Description

Our client, based in Sligo, have an urgent requirement for a Project Engineer on a 12 month daily rate contract. This is an excellent opportunity to join one of the leading pharmaceutical companies in the North West.

The successful candidate's role will involve working within the Engineering Function to develop a culture of accountability, empowerment, continuous improvement, customer focus, collaboration, involvement and development of oneself within the Site.
Driving continuous improvement. Support communication and material flow between the Engineering Function and the Value Streams.

Responsibilities:
* Provide technical and engineering expertise to support new equipment and process introduction, changes to existing equipment and processes.
* Manage Engineering Change Controls in compliance with GMP and regulatory requirements. Person must ensure all projects comply to applicable codes, accepted engineering practices, and GES standards
* At all times this person needs to reflect the Sligo site goals of cost competitiveness, working to ensure world class NPI capability and helping to drive step change in OEE performance.
* Provide technical support for the modification of existing operations equipment and processes ensuring compliance with current regulatory and technical regulations.
* Generating User Requirement Specifications/Functional Design specifications, IQ, OQ, PQ documentation for projects.
* Prepare engineering project proposals and budgets, using tools such as FMEA to identify risks, monitor budgets and track trends. Review and approve project Contractor invoices.
* Monitoring outside ESPs when on-site, recording/copying licenses, permits and Safe Pass cards etc, and ensuring all ESP practices are safety and quality compliant.
* Perform duties in a compliant manner and behave in accordance with our Quality Management System requirements.
* Maintain your area of responsibility in an inspection ready state ensuring quality and GMP standards are maintained appropriate to your role.

Requirements
* Minimum of 2 years experience in an engineering role within a Pharmaceutical / Medical Devices / GMP environment.
* Ability to see the bigger picture. Good understanding of relationship between quality and operations.
* Previous experience in leading projects.
* Engage in / lead design of solutions and improvements.
* Good working knowledge of Microsoft packages and Autocad.

If you feel you are a food fit for this position please apply directly or contact Derek Sheridan on for further information

To find out more about Real please visit www.realstaffing.com
Start date
07/2013
Duration
12 months
From
Real Staffing
Published at
13.07.2013
Project ID:
566863
Contract type
Freelance
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